- Research article
- Open Access
Genome-wide analysis of lectin receptor-like kinases in Populus
BMC Genomics volume 17, Article number: 699 (2016)
Receptor-like kinases (RLKs) belong to a large protein family with over 600 members in Arabidopsis and over 1000 in rice. Among RLKs, the lectin receptor-like kinases (LecRLKs) possess a characteristic extracellular carbohydrate-binding lectin domain and play important roles in plant development and innate immunity. There are 75 and 173 LecRLKs in Arabidopsis and rice, respectively. However, little is known about LecRLKs in perennial woody plants.
Here we report the genome-wide analysis of classification, domain architecture and expression of LecRLKs in the perennial woody model plant Populus. We found that the LecRLK family has expanded in Populus to a total of 231, including 180 G-type, 50 L-type and 1 C-type LecRLKs. Expansion of the Populus LecRLKs (PtLecRLKs) occurred partially through tandem duplication. Based on domain architecture and orientation features, we classified PtLecRLKs into eight different classes. RNA-seq-based transcriptomics analysis revealed diverse expression patterns of PtLecRLK genes among leaves, stems, roots, buds and reproductive tissues and organs.
This study offers a comprehensive view of LecRLKs in the perennial woody model plant Populus and provides a foundation for functional characterization of this important family of receptor-like kinases.
Cell-surface receptors play important roles in perceiving and processing signals at the cellular level. One large family of such cell-surface receptors are the receptor-like kinases (RLKs) [1, 2]. There are over 600 RLKs in Arabidopsis and over 1000 in rice . The role of RLKs as cell-surface receptors perceiving extracellular signals has been validated through functional characterization of several RLK members, e.g., receptor-like Ser/Thr kinases BRASSINOSTEROID-INSENSITIVE 1  and CLAVATA1 . RLKs are typically comprised of an N-terminal extracellular domain, an intermediate transmembrane domain and a C-terminal kinase domain. A total of 15 subfamilies of RLKs have been classified on the basis of their extracellular domains .
The lectin receptor-like kinases (LecRLKs) are defined by their characteristic extracellular lectin domain that resembles carbohydrate-binding lectin proteins in humans and animals [5, 6]. However, no LecRLK has been found in the genomes of human or yeast and LecRLKs are viewed as plant-specific [7, 8]. LecRLKs have been best characterized in the two model plant species, Arabidopsis and rice. There are a total of 75 and 173 LecRLKs in Arabidopsis and rice, respectively . Available evidence suggested that LecRLK genes are also present in many other plant species including Nicotiana benthamiana, Solanum lycopersicum, Arabidopsis lyrata, Glycine max, Medicago truncatula, Zea mays and Sorghum bicolor [9–11]. Although the number is low, LecRLK genes also exist in the non-vascular and non-seed baring plants, e.g., Physcomitrella patens and Selaginella moellendorffii, respectively . LecRLKs are further classified into three different forms, i.e., G-type, L-type and C-type, based on the lectin domain identity. There are 32 G-type, 42 L-type and 1 C-type LecRLKs in Arabidopsis, and 100 G-type, 72 L-type and 1 C-type LecRLKs in rice . The G-type LecRLKs were known as B-type LecRLKs due to the resemblance of their extracellular domain with the bulb-lectin proteins in humans and animals [5, 12]. G-type LecRLKs are also known as S-domain RLKs due to the presence of an S-locus domain known to be involved in pollen self-incompatibility [13–16]. The lectin domains of G-type LecRLKs possess a β-barrel structure and are predicted to bind to α-D-mannose. Many G-type LecRLKs also contain a cysteine-rich epidermal growth factor (EGF) domain and a plasminogen/apple/nematode (PAN) domain [8, 17]. The EGF domain is predicted to be involved in the formation of disulfide bonds and the PAN domain is believed to be involved in protein-protein and protein-carbohydrate interactions . It should be noted that EGF and PAN domains are only found in the G-type and are absent in the L-type and C-type LecRLKs. The L-type LecRLKs contain a characteristic legume-lectin domain that is believed to exhibit glucose/mannose-binding specificity ; the C-type LecRLKs contain a calcium-dependent carbohydrate-binding lectin domain.
Substantial evidence suggests that LecRLKs play important roles in plant development and innate immunity [17, 20]. However, most studies on LecRLKs were performed in the herbaceous plants. Little is known about LecRLKs in the perennial woody plants which are of significant importance to carbon sequestration, global carbon cycling, environmental and ecological systems and biomass production for forestry and bioenergy industries. Populus is a model species for perennial woody plants but there are only a few early studies reporting on the presence of LecRLKs [21–23]. A comprehensive view of LecRLKs in this perennial woody model plant is still lacking. Here we report the genome-wide analysis of classification, domain architecture and expression of LecRLKs in Populus.
LecRLK sequence homolog search in Populus
Populus LecRLK (PtLecRLK) amino acid sequences were collected from v3.0 Populus trichocarpa gene annotation curated in the Phytozome (v11.0) database managed by Joint Genome Institute (JGI; www.phytozome.jgi.doe.gov). To identify G-type PtLecRLKs, AT1G65790 (a G-type Arabidopsis LecRLK) was used as a query to collect its Populus homologs by dual-affine smith-watermann alignments integrated in Phytozome . We only accepted PtLecRLKs having over 30 % amino acid sequence similarity in the initial alignment. Then, we performed the reciprocal alignment analysis using the Populus LecRLK protein (Potri004G028000) showing highest amino acid sequence similarity with AT1G65790 as the input to search for additional potential Populus homologs.
The same process was performed to identify L-type and C-type PtLecRLKs using AT2G37710 and AT1G52310 as primary input query, respectively. The L-type PtLecRLK showing highest amino acid sequence similarity with AT2G37710, Potri006G088400, was then used as a template to search for additional potential Populus homologs.
In case of isoform information among collected amino acid sequences, the longest full-length amino acid sequences were selected and used for further analyses. These full-length amino acid sequences were subjected to Chromosome Digram module integrated in POPGENIE (popgenie.org) to generate PtLecRLK loci location on Populus chromosomes .
LecRLK sequence homolog search in moss, shrub, soybean and Eucalyptus
To identify LecRLKs in another woody plant, we searched Eucalyptus grandis v2.0 genome in phytozome v11.0 by using the same approach that was taken to identify PtLecRLKs. For the identification of G-type LecRLKs in Eucalyptus, we performed amino acid sequence alignment using AT1G65790 (a G-type Arabidopsis LecRLK) as the initial query. We collected Eucalyptus homologs with over 30 % similarity at the amino acid level with AT1G65790. A second round of protein homolog search was performed by using Potri.004G028000 (a PtLecRLK showing highest amino acid sequence similarity with AT1G65790) as a new input to identify additional potential G-type Eucalyptus LecRLKs (EgLecRLKs). Finally, we used Eucgr.D00925, the protein showing highest amino acid similarity with Potri.004G028000, as a template to identify other potential homologs.
To search for L-type and C-type EgLecRLKs, AT2G37710 and AT1G52310 were used as the template, respectively. Then, we used Potri.006G088400 that shows highest amino acid sequence similarity (70 %) with AT2G37710 as a template to identify additional potential homologs of L-type EgLecRLKs. Potri.001G062300, the unique C-type PtLecRLK and the homolog of AT1G52310, was used as a template to confirm the identification of C-type EgLecRLK.
We also extended our search for LecRLKs in moss (Physcomitrella patens, v3.3), shrub (Amborella trichopoda, v1.0), corn (Zea mays, Ensembl-18) and soybean (Glycine max, Wm82.a2.v1). We used the same protocol and the same representative Populus proteins. Due to the evolutional distance of moss genome, we used 40 % similarity as a threshold to collect the full-length amino acid sequences of moss LecRLKs. For C-type LecRLK analysis, single gene was identified from grape (Vitis vinifera, Genescope.12X) genome by the same protocol.
Functional domain annotation and functional motif prediction of PtLecRLKs
To predict protein functional motifs and domains, including specific lectin and protein kinase domains, the full-length amino acid sequences of PtLecRLKs were subjected to Pfam v29.0 (http://pfam.xfam.org) , ScanProsite v20 (http://prosite.expasy.org/scanprosite/)  and InterPro v56.0 (https://www.ebi.ac.uk/interpro/)  based on HMMER . Since some motifs such as Legume lectin and EGF motif were not predicted in ScanProsite, we merged those annotation results to generate a protein domain structure containing all predicted protein functional domains. From them, we filtered out the protein sequences missing either lectin or kinase domain for further analysis.
To assess the location and number of transmembrane domain (TM), the full-length amino acid sequences used for alignment and phylogenetic analysis were subjected to TMHMM web-based software (v2.0) (www.cbs.dtu.dk/services/TMHMM) . This software also provided the information on membrane transpassing pattern. Significant TM prediction was determined by selecting the probability score ≥ 0.8.
Signal peptide on amino acid sequence was predicted by SignalP v4.0 , under a valuable signal sequence selection score ≥ 0.7. When the TM motif was predicted as potential signal peptide, the priority was given to signal peptide prediction.
Amino acid sequence alignment and phylogenetic analysis
Phylogenetic and amino acid sequence alignment analyses of collected full-length PtLecRLKs were conducted on Geneious R8 software platform (v8.1.2; Biomatters Ltd., New Zealand). The amino acid sequence identity of PtLecRLKs was calculated by ClustalW integrated in Genious R8. ClustalW alignment was run under the typical options composed of BLOSUM 62 cost matrix with the penalty of gap open cost 10 and gap extend cost 0.2. To build phylogenetic tree, the same set of PtLecRLK amino acid sequences were subjected to MUSCLE (v 3.5) by 12 maximum number of iterations together with kmer6_6 for distance measurement under Neighbor-joining clustering method . The best fitting model for each phylogenetic tree construction was performed with MUSCLE alignment result by model selection (ML) method integrated in MEGA7 (v 7.0.18) . We applied the best fitting model for phylogenetic tree by selecting the model having the lowest value of Akaike information criterion (AIC), Bayesian information criterion (BIC), and maximum likelihood (InL) values. To construct the best phylogenetic tree, we performed PHYML method with the best fitting model for each phylogenetic tree . The information of the best fitting model was described in each figure legend of phylogenetic tree. Nearest-Neighbor-Interchange (NNI) was used as a heuristic to improve the likelihood tree.
To validate the phylogenetic tree, we rebuilt another phylogenetic tree by using the neighbor-joining method integrated in Genious software with Jukes-Cantor genetic distance model using bootstrap 1000 replicates resampling to assess statistical strength of phylogenetic tree with the same MUSCLE alignment .
Analysis of gene expression of PtLecRLKs
To compare the expression of PtLecRLKs in different tissues and developmental stages, we compiled the expressed values of PtLecRLK genes from RNA-seq data in different tissues under standard or treatment conditions from the Populus Gene Atlas Study at Phytozome (www.phytozome.jgi.doe.gov). Normalized fragments per kilobase of transcript per million mapped reads (FPKM) values were compared to determine gene expression in different tissues. Collected data was summarized by heatmap function in ggplot2 R package . To verify the expression of PtLecRLKs identified in the Gene Atlas Study, RT-PCR was performed with gene-specific primers for six PtLecRLK genes and the PtUBCc as an internal control. All primers used for RT-PCR analysis are listed in the Additional file 1. The same tissues of root tip and root without root tip, internode and node of stem, and young leaf tissue that were originally used for RNA extraction at Oak Ridge National Laboratory for RNA-seq at JGI in the Populus Gene Atlas Study were used for RNA extraction for RT-PCR analysis. Total RNA was extracted from adopted tissues with PureLink Plant RNA reagent (Ambion™, Austin, TX) followed by RNA purification with Spectrum Plant RNA purification kit following the manufacturer’s protocol (Sigma-Aldrich, St. Louis, MO). One μg of total RNA was used to synthesize complementary DNA (cDNA) by reverse transcription with Revertaid reverse transcriptase (Thermo Fisher Scientific, Waltham, MA). Ten ng of reversely transcribed cDNA was used to perform PCR reaction with the gene-specific primers in the PCR reaction mixture of DreamTaq Green PCR Master Mix (Thermo Fisher Scientific, Waltham, MA). The PCR reaction was performed with the program consisting of a pre-denaturation at 95 °C for 2 min, 30 cycles of the reaction of 95 °C for 30 s, 57 °C for 30 s and 72 °C for 30 s. Another step of 72 °C for 7 min was followed for the final extension. The PCR amplification results were run on 1 % agarose gel. The gel image was taken by using ChemiDoc XRS+ image analysis system (Bio-Rad, Hercules, CA).
Populus LecRLKs identification and classification
The full-length amino acid sequences of three representative Arabidopsis LecRLKs (G-type: AT1G65790; L-type: AT2G37710; C-type: AT1G52310) were used initially as templates to search for their sequence homologs encoded by the genome of Populus trichocarpa (hereafter refer as Populus). To identify additional potential homologs, the Populus proteins showing highest amino acid sequence similarity with the corresponding G-, L- and C-type Arabidopsis LecRLKs were then used as templates to search the Populus genome again. The search identified a total of 231 unique loci encoding LecRLKs in Populus (Table 1). We refined our search criteria to identify only LecRLKs that contain both a lectin domain and a kinase domain. These proteins were then classified as G-type, L-type and C-type PtLecRLKs on the basis of the identity of lectin domain. It should be noted that there were a number of proteins that contain a lectin domain but lacks a kinase domain (Additional file 2). For example, proteins encoded by Potri.010G005900 and Potri.010G017400 contain only a bulb (mannose binding) lectin domain, and as such, did not meet our criteria of being LecRLKs and were not considered in subsequent analyses.
In order to validate the classification of PtLecRLKs into alternate types, we performed three independent analyses using full-length amino acid sequences; i.e., i) amino acid sequence alignment; ii) amino acid identity and iii) phylogenetic analysis. We first analyzed randomly selected proteins, three each from G- and L-type, plus the sole C-type PtLecRLK. As shown in the Additional file 3, the lectin domain regions were distinct from each other whereas the protein kinase domains were highly conserved. The phylogenetic analysis with full-length amino acid sequences revealed that members from each type formed separate clades, with the L-type PtLecRLKs showing at least 47 % amino acid identity each other and the G-type showing at least 66 % amino acid identity between currently selected proteins (Additional file 3). On the basis of these results, phylogenetic analysis was performed with full-length amino acid sequences of all 231 PtLecRLKs. As shown in Fig. 1, three different types of PtLecRLKs were clearly separated in three different clades.
In total, 231 PtLecRLKs with 180 G-type, 50 L-type and 1 C-type were identified (Table 1; Additional files 4, 5 and 6). The total number of LecRLKs in Populus (231) is about three times that in Arabidopsis (Table 1). Comparison between the numbers of LecRLKs in these two dicot species also revealed that the number of G-type LecRLKs in Populus is larger than L-type (G-type: 180 vs L-type: 50) whereas in Arabidopsis , there are more L-type than G-type LecRLKs (G-type: 32 vs L-type: 42). Interestingly, there are also more G-type than L-type LecRLKs in rice (G-type: 100 vs L-type: 72), similar to that in Populus. However, although the total number of LecRLKs in Populus is larger than that in rice, Populus has fewer L-type LecRLKs than rice (Table 1).
To extend our analysis to other woody species, we performed genome-wide search for LecRLKs in the Eucalyptus genome by the same approach that we used for identifying PtLecRLKs. In addition, we searched LecRLK distribution in four more species including moss, shrub, corn and soybean. In total, we identified 198 EgLecRLKs (G-type: 118, L-type: 79, C-type: 1) (Table 1; Additional file 7). Soybean has 189 LecRLKs (G-type: 123, L-type: 64, C-type: 2). Similar to Populus, Eucalyptus and soybean also have more G-type LecRLKs than L-type. In shrub and corn, a total of 56 (G-type: 25, L-type: 30, C-type: 1) and 95 (G-type: 46, L-type: 48, C-type: 1), respectively, were identified. Moss has only 5 LecRLKs. All tested genomes have one or two C-type LecRLK (Table 1; Additional file 7). Taken together, these results suggest that the G-type LecRLKs have been disproportionately expanded in Populus, compared to Arabidopsis. On the other hand, Populus contains only one C-type LecRLK, identical to that in Arabidopsis, rice and Eucalyptus.
Tandem repeats and size difference of PtLecRLKs
Among 231 PtLecRLKs, a total of 195 PtLecRLK loci were distributed across most Populus chromosomes; 36 PtLecRLK genes were annotated on scaffolds with an indeterminate chromosomal location. Of the 195 PtLecRLK genes, approximately 38 % of the G-type PtLecRLKs were found as clusters of tandem repeats (Fig. 2a). In some chromosomal locations on chromosome 1, 10, and 11, there were more than 20 PtLecRLK genes clustered together (named “super tandem repeat region” here) (Fig. 2b-d). This tandem repeat feature is similar to that reported in Brassicaceae and related outgroups  and is likely a major attributor for the G-type LecRLK family expansion.
Maximum likelihood tree of G-type PtLecRLKs showed that tandem repeat genes on chromosome 10 were clustered in the same clade (Fig. 3a). PtLecRLK tandem repeat genes in the super tandem repeat regions of chromosome 1 were clustered in several neighboring clades (Fig. 3a). Twelve out of 29 tandem repeat genes on chromosome 11 also occurred in an alternate clade that was clearly separated from the clade with the rest of genes (light blue: chromosome 1, light green: chromosome 10, and light red: chromosome 11; Fig. 3a). Unlike G-type PtLecRLKs, the only tandem repeat region for L-type PtLecRLKs was found in the chromosome 9 where a total of 8 L-type PtLecRLKs were clustered together (Fig. 3b).
By examining amino acid number in each PtLecRLK, we found that G-type PtLecRLKs are generally larger than L-type and C-type, with the average of 806 amino acids versus 645 in L-type and 544 in C-type (Fig. 2e). This is largely due to the fact that in addition to the lectin domain, G-type PtLecRLKs often contain the EGF and PAN domains as well as the S-locus glycoprotein domain. In addition, some G-type PtLecRLKs contain a DUF3403 domain in the C-terminus, posterior to the kinase domain. The largest PtLecRLK (Potri.T084700) has 1473 amino acids.
Phylogenetic analysis of PtLecRLKs
To perform the phylogenetic tree analysis, maximum likelihood tree was constructed from alignment result using full-length amino acid sequences of PtLecRLKs. For G-type phylogenetic tree construction, an Arabidopsis lectin 3.1 (AT3G15356; L-type LecRLK) was used as an unrelated protein. This protein was also used as an outgroup in the previous phylogenetic analysis of Arabidopsis and rice G-type LecRLKs . In addition, 8 G-type Arabidopsis LecRLKs that were classified as the representative genes in each group in phylogenetic tree  were subjected together with 180 G-type PtLecRLKs to build a phylogenetic tree. The phylogenetic tree of G-type PtLecRLKs was constructed and clustered into several groups. The grouping was done in a manner similar to what was done for Arabidopsis and rice LecRLKs . These 180 G-type PtLecRLKs were divided into 8 large cluster groups (Fig. 3a). Based on distinct clade formation, the group VIII was subdivided into 9 different subgroups (VIII-a to VIII-i). All those super tandem repeated PtLecRLKs were categorized in group VIII as highlighted by different color (light blue: chromosome 1, light green: chromosome 10, and light red: chromosome 11; Fig. 3a). Group III to VII clades did not contain any Arabidopsis G-type LecRLKs.
Through the same process, 50 L-type PtLecRLKs were subjected to phylogenetic analysis. Two distant Arabidopsis proteins, PEPK1 and WAK1, and 14 Arabidopsis L-type LecRLKs that were reported as the representative L-type AtLecRLKs in each group were used to define each clade [8, 37]. Based on the full-length amino acid sequence alignment of L-type PtLecRLKs with Arabidopsis proteins, the maximum likelihood phylogenetic tree showed nine major groups that are classified by different clade separation (Fig. 3b). Group IV was divided into two subgroups. This is also supported by the phylogenetic analysis of additional L-type LecRLKs from Eucalyptus (Fig. 4b). Each group clade, except group III of singleton clade, contains at least one Arabidopsis L-type LecRLK (Fig. 3b).
The constructed phylogenetic trees of G- and L-type PtLecRLKs were validated by a different phylogenetic method using neighbor joining with 1000 bootstraps (Additional file 8). Most clade formations were similar between these two methods except minor differences in clustering. For example, group VIII-f merged into group VIII-h clade in neighbor joining phylogenetic tree (Additional file 8). Nonetheless, PtLecRLKs were consistently formatted into the same clade by using these two different methods for phylogenetic tree construction (Fig. 3, Additional file 8).
To assess whether the PtLecRLKs were evolutionally separated from LecRLKs in a different woody plant species, we compiled LecRLKs from Eucalyptus grandis v2.0 genome in Phytozyme v11.0. Eucalyptus genome has a total of 198 EgLecRLKs (118 G-type, 79 L-type, and 1 C-type). For G-type LecRLK amino acid sequence alignment and phylogeny analysis, 180 G-type PtLecRLK were analyzed together with 118 G-type EgLecRLKs, 8 representative Arabidopsis LecRLKs  including a distant Arabidopsis protein (AtLec3.1), and 13 rice representative G-type LecRLKs that were used as the representative members in each group to classify rice G-type LecRLKs . Although we included Eucalyptus and rice LecRLKs in the analysis, typical nodes or branches shown in this tree (Fig. 4a) is similar to the tree constructed using Populus and Arabidopsis LecRLKs (Fig. 3a). The groups VII and VIIIf-h clades were only shared by G-type LecRLKs from woody plants without LecRLKs from herbaceous plants (Fig. 4a). This observation was consistent with the phylogenetic trees built by a different tree building method (Geneious tree builder) using neighbor joining method with 1000 bootstrap resampling (Additional file 9). This phylogenetic tree showed that three genes of group II were divided into different new clades. Group VI was also divided into two different clades. Except for these two minor differences, the clustering and grouping results were almost identical between these two methods for phylogenetic tree construction.
Same analysis was performed for L-type LecRLKs by using all 50 PtLecRLKs together with all 79 EgLecRLKs, 14 AtLecRLKs identified as the representative genes of each group in the published study , and 9 rice LecRLKs identified as the representative genes of each group in rice L-type LecRLK analysis in the published study . The maximum likelihood phylogenetic tree showed that the singleton clade of Group III shared its clade with four G-type EgLecRLKs (Fig. 4b). Group IV-b was also divided to two clades with EgLecRLKs (Fig. 4b). All nine representative rice L-type LecRLKs were integrated into group VIII. This clade was distinctly separated from L-type LecRLKs from other species (highlighted by light blue; Fig. 4b). The clade next to group VIII was the largest cluster consisting of only EgLecRLKs (Fig. 4b). In total, three distinct clades were associated with EgLecRLKs only (highlighted by light red; Fig. 4b). Again, this pattern was also observed in the tree constructed by using the neighbor joining with 1,000 bootstrap resampling method (Additional file 9).
In the case of C-type LecRLK, we identified single C-type LecRLK in Populus, Eucalyptus, Arabidopsis and rice genomes by amino acid sequence alignment with Arabidopsis C-type LecRLK. To examine whether C-type LecRLK is also present as a single copy in other species, we extended our search to moss (Physcomitrella patens), shrub (Amborella trichopoda), corn (Zea mays), soybean (Glycine max) and grape (Vitis vinifera). Single copy of C-type LecRLK was identified in the grape, corn and shrub genomes whereas moss and soybean had two C-type LecRLKs. To examine the evolutional relationship of C-type LecRLK, we constructed phylogenetic tree with full-length amino acid sequences of C-type LecRLKs. The clade containing moss C-type LecRLKs was placed far away from other land plant species. C-type LecRLKs of shrub is closer with that of monocot plant than dicot woody and herbaceous plants (Fig. 4c). The phylogenetic tree using neighbor-joining method also showed a similar pattern (Additional file 9).
Domain architecture of PtLecRLKs
As noted above, G-type PtLecRLKs often contain mannose binding bulb-lectin domain, S-locus glycoprotein domain, EGF domain, PAN domain and DUF3403 domain and thus having more diverse domain architectures. Within G-type, there are 31 PtLecRLKs that contain all these five domains; only 16 G-type PtLecRLKs contain a single domain, the bulb-lectin domain (Fig. 5). A total of 159 out of 180 G-type PtLecRLKs contain the S-locus glycoprotein domain. Some unique domain architectures were also observed within the G-type PtLecRLKs. For example, one G-type PtLecRLK (Potri.004G061900) contains two tandem bulb-lectin domains. Another G-type PtLecRLK (Potri.011G038000) contains two S-locus protein domains and two PAN domains (Fig. 5). The largest G-type PtLecRLK (Potri.T084700) appears to be a fusion protein of two PtLecRLKs with two bulb-lectin domains and two kinase domains (Fig. 5). A prokaryotic lipoprotein lipid attachment motif was identified in a G-type PtLecRLK, Potri.011G03880 (Fig. 5), implying that this protein is potentially subjected to post-translational modification for membrane localization. A total of 83 G-type PtLecRLKs contain the DUF3403 domain at their C-terminus, posterior to the protein kinase domain (Fig. 5). This DUF3403 domain has also been reported in LecRLKs from other plant species [10, 38] but its function is unknown.
Four G-type PtLecRLKs have the truncated lectin domain, lacking at least 10 amino acids, and 7 other G-type PtLecRLKs have a truncated protein kinase domain (Additional file 10). In addition, we identified three highly conserved motifs in the bulb lectin domain and two cysteine-rich motifs (C-rich), localized in the C-terminal region of EGF motif and the middle of PAN domain (Additional file 10).
Compared with G-type, the domain architecture of L-type and C-type PtLecRLKs are less complex (Fig. 5). All L-type PtLecRLKs contain a single legume lectin domain. However, six L-type PtLecRLKs had a truncated legume lectin domain and 4 others lack middle portion of conserved protein kinase domain (Additional file 11). In addition, we identified three highly conserved motifs in the legume lectin domain of L-type PtLecRLKs (Additional file 11).
Domain orientation of PtLecRLKs
RLKs are typically comprised of an extracellular domain, a TM and an intracellular kinase domain. Our analysis of the TM domain, however, has revealed several interesting features for PtLecRLKs. We identified PtLecRLKs with diverse domain orientation features and classified them into eight different classes based on computational approaches of Krogh et al. . These eight different classes were first grouped on the basis of the number of TM domains, and then further separated by the position of lectin domain and kinase domain (Fig. 6). Class I to III PtLecRLKs have one, Class IV to Class VI have two, and Class VII and Class VIII have three TM domains. Class I PtLecRLKs have a typical extracellular lectin domain and an intracellular kinase domain (i.e., Potri.001G41300) (Fig. 6); there are 24 G-type and 15 L-type PtLecRLKs falling into the Class I category (Table 2). Class II G-type PtLecRLKs have a reversed extracellular kinase domain and an intracellular lectin domain (i.e., Potri.005G014700), opposite of Class I; there are 100 G-type proteins in this category, representing the largest group of G-type PtLecRLKs. Class III PtLecRLKs have an extracellular lectin domain and an extracellular kinase domain (i.e., Potri.001G412300). Class IV PtLecRLKs also have both extracellular lectin domain and extracellular kinase domain but these domains are separated by two inverted TM domains (i.e., Potri.013G115800). Class V PtLecRLKs have an extracellular kinase domain and an intracellular lectin domain with two inverted TM domains (i.e., Potri.019G120000). Class VI PtLecRLKs have an extracellular lectin domain and an intracellular kinase domain with two inverted TM domains (i.e., Potri.011G033400), opposite of Class V. Class VII PtLecRLK has two extracellular lectin domains and two kinase domains with three TM domains (i.e., Potri.T084700), resembling the fusion of two Class I PtLecRLKs. Class VIII PtLecRLK has an intracellular lectin domain and an extracellular kinase domain with three TM domains (i.e., Potri.011G128600). Class VII and VIII PtLecRLKs (with three TM domains) were only identified in G-type PtLecRLKs. It should be noted that such unusual domain orientation has been reported in LecRLKs in other plant species , but appeared to be more abundant in Populus.
Although L-type PtLecRLKs have much simpler domain architecture than G-type, 8 out of 50 L-type PtLecRLKs contain two TM domains (Table 2; Additional file 5). Twenty-nine L-type PtLecRLKs were grouped in Class I and Class II (Table 2; Additional file 5). The single C-type PtLecRLK was in Class II (Table 2; Additional file 6). It should be noted that not all PtLecRLKs were predicted to contain the TM domain. TM was not found in 33 G-type and 12 L-type PtLecRLKs (Additional files 4, 5, 10 and 11). The complete domain architecture and orientation of G-, L- and C-type PtLecRLKs are listed in Additional files 4, 5 and 6, respectively.
Expression patterns of PtLecRLK genes
Little is known about the function of LecRLKs in Populus. As the first attempt to provide insights into their potential functions, we analyzed the expression of PtLecRLK genes across various tissues and organs by mining RNA-seq data from the Populus Gene Atlas Study in Phytozome v11.0 (http://phytozome.jgi.doe.gov). In this study, there are 24 different samples including samples collected under standard and treatment conditions. We complied the FPKM values of PtLecRLK genes in three different types detected in 24 different samples in the Additional files 12, 13 and 14. We also generated heatmap image of 231 PtLecRLK genes collected from 12 different samples under standard conditions (Fig. 7). These datasets contain four different tissue types of different growth stages including two root samples (root and root tip), three leaf samples (immature, first fully expanded and young), two stem samples (internode and node), and five bud samples (early dormant, fully open, late dormant, predormant I and predormant II stage). A large number of PtLecRLK genes (G-type: 59; L-type: 19) showed low (FPKM < 1) or undetectable expression (FPKM = 0) in the interrogated tissues (Fig. 7, designated zone I). A total of 28 PtLecRLK genes (G-type: 13, L-type: 14, and C-type: 1) showed expression across all tissues (Fig. 7, zone II). A total of 22 PtLecRLK genes (G-type: 16; L-type: 6) showed root-specific expression (Fig. 7, zone III) (Additional file 15). The bud tissues had the largest number of tissue-specific PtLecRLK genes with 41 G-type and 4 L-type (Fig. 7, zone IV; Table 3). Three genes including Potri.011G033400, Potri.013G095800 and Potri.010G015400 were expressed solely in the stem tissues. A G-type PtLecRLK gene was expressed specifically in the leaf tissues with FPKM value close to 1 (Table 3; Additional file 12). In the analysis of reproductive tissues/organs from female and male Populus trees, we observed that 21 G-type and 9 L-type PtLecRLK genes were specifically expressed in female reproductive tissues/organs. Nine G-type and 1 L-type PtLecRLK genes were expressed only in male reproductive tissues/organs (Additional files 16 and 17). The sole C-type PtLecRLK gene was expressed across all tissues examined (Fig. 7c; Additional file 14). The distribution of the number of PtLecRLK genes from each group expressed in different tissues and organs is summarized in the Additional file 18. In general, no any group of PtLecRLK genes was uniquely expressed in a given tissue or organ.
To verify the Gene Atlas dataset and tissue-specific gene expression in the tested tissues, we performed RT-PCR analysis with gene-specific primers using cDNA generated from two root samples, one leaf sample, and two stem samples that were used for the Populus Gene Atlas Study. Two genes from L-type and three genes from G-type, which were detected with higher FPKM value in root tissue than other tissues, were tested together with the sole C-type PtLecRLK. Consistent with the RNA-seq data, C-type PtLecRLK was detected across roots, leaf and stems (Fig. 7d). Potr.007G004200, an L-type PtLecRLK, was detected in root tissues only. The other L-type PtLecRLK, Potri.001G455500, was detected in root tissues and also weakly in two stem tissues (Fig. 7d). No transcript of these two L-type PtLecRLK genes was detected in young leaf tissues, which is consistent with Gene Atlas dataset (Additional file 13). For G-type PtLecRLKs, three tested genes were only detected in the root tissues (Fig. 7d). Taken together, the results from the RT-PCR analysis was largely consistent with the Gene Atlas data.
The membrane-bound LecRLKs are believed to play important roles in the cellular responses to external stimuli including pathogen attack, environmental stress and developmental clues [17, 20]. Current literatures reporting the classification and function of LecRLKs have been limited in herbaceous plant including Arabidopsis, tobacco, rice and tomato [8, 36, 37]. In this study, we identified 180 G-type, 50 L-type and 1 C-type LecRLKs in the perennial woody model plant Populus trichocarpa. Our studies revealed several important features of LecRLKs in Populus.
Expansion of LecRLKs in Populus
Comparison of the total number of different types of LecRLKs among Arabidopsis, rice, corn, shrub, soybean, Eucalyptus and Populus revealed that the number of G-type LecRLKs differed drastically among these species (Table 1), and that in Populus, G-type LecRLKs have expanded. This notion is supported by the analysis of LecRLKs in another woody species, Eucalyptus. We identified a total of 118 G-type EgLecRLK out of 198 EgLecRLKs (Table 1; Additional file 7). Moreover, it was previously reported that the L-type LecRLKs were expanded than G-type LecRLKs in Arabidopsis . However, in Populus, the number of G-type LecRLKs is over three times that of L-type LecRLKs (Table 1). Because the majority (>88 %) of G-type PtLecRLKs contains the S-locus glycoprotein domain which is an essential domain for sporophytic self-incompatibility response-related proteins, the difference in the number of G-type LecRLKs between Arabidopsis (G-type: 32 vs L-type: 42) and Populus (G-type: 180 vs L-type: 50) may be partially explained by the fact that Arabidopsis is a self-fertile plant whereas Populus is an obligate outcrossing plant. Because LecRLKs are predominantly hypothesized to participate in biotic stress tolerance [12, 37, 38], the large number of LecRLKs in Populus may also suggest that perennial plants have evolved a large array of LecRLKs in response to longer life cycles and larger probability of exposure to more diverse microbial populations.
Based on phylogenetic analysis of full-length amino acid sequences of LecRLKs from Populus, Arabidopsis, Eucalyptus and rice, both G-type and L-type LecRLKs have the divergent group only associated with two woody species, implicating that woody plant LecRLKs may have evolved divergent functions than herbaceous plants (Fig. 4; Additional file 9). Interestingly, a major part of Eucalyptus L-type LecRLKs formed a unique clade next to PtLecRLKs (Fig. 4b; Additional file 9).
A total of 56 G-type PtLecRLK genes were expressed in the reproductive tissues/organs of female and male Populus plant (Additional file 17). Among them, 21 G-type PtLecRLK genes were specifically expressed in female reproductive tissues/organs whereas 9 G-type PtLecRLK genes were specifically expressed in the male. It should be noted that the S-locus domain localized typically on G-type LecRLKs was initially reported as the pollen factor inducing the rejection of self-pollen in the self-incompatibility process . Since Populus is a dioecious species, S-locus domain-containing LecRLKs are likely to have evolved new functions beyond its identified function in self-incompatibility.
Tandem repeats of PtLecRLKs
A total of 195 out of 231 PtLecRLK loci were assigned with chromosomal location and were distributed on most Populus chromosomes. Similar to what has been reported in other plant genomes [36, 37], PtLecRLKs were found in tandem repeats in many chromosomes. Three super tandem repeat regions of G-type PtLecRLK genes were identified in chromosomes 1, 10 and 11 (Fig. 2). These super tandem duplicate gene clusters generally have high phylogenetic proximity each other as shown in the phylogenetic analysis (Fig. 3a). Interestingly, the super tandem repeat genes of G-type PtLecRLKs in chromosome 11 and 1 were less strictly clustered, implying that these PtLecRLKs may have evolved different functions. These tandem duplicated genes do not appear to be derived from the Salicoid whole-genome duplication event , such that, the super tandem repeat region identified in the chromosome 10 (all G-type PtLecRLKs in this region) was absent on the chromosome 8 (Fig. 2).
Domain architecture and organization of PtLecRLKs
By analyzing the predictions of domain architecture and organization, we observed several interesting features of PtLecRLKs. Firstly, in addition to the bulb lectin domain, G-type PtLecRLKs often contain other domains including S-locus glycoprotein domain, EGF domain, PAN domain and DUF3403 domain. A total of 31 G-type PtLecRLKs contain all of these five domains. The DUF3403 domain was found in 83 G-type PtLecRLKs at their C-terminus posterior to the protein kinase domain (Fig. 5). LecRLKs are typically composed of an extracellular lectin domain and an intracellular PK domain, and in our study, we were able to classify PtLecRLKs into 8 classes on the basis of TM domain predictions and found that most PtLecRLKs belongs to the single TM protein group (Classes I, II and II), thereby functioning as potential membrane bound receptors. However, we also identified a number of PtLecRLKs with two or three TM domains (Fig. 6 and Table 2). Surprisingly, unlike reports from herbaceous plants, there are more PtLecRLKs predicted to have an intracellular lectin domain and an extracellular protein kinase domain than PtLecRLKs with an extracellular lectin domain and an intracellular protein kinase domain (Table 2). The functional significance of these observations remains undefined.
Two cysteine-rich motifs were identified in the C-terminal region of EGF motif and the middle of PAN domain of G-type PtLecRLKs (Additional file 10). These motifs may serve as potential protein-protein interaction sites. A number of PtLecRLKs did not contain the TM domain (Additional files 4 and 5). Therefore, the action of such proteins may not be restricted to signal detection at the cell surface and may function in a non-membrane bound context. Finally, a number of proteins with bulb lectin domain and legume lectin domain, but without the kinase domain, were identified (Additional files 2 and 19). Interestingly, some of these proteins also contain the EGF, PAN or DUF3403 domain (Additional files 2 and 19). The transcript of genes encoding these lectin domain-containing proteins were detected in the Populus Gene Atlas (data not shown), suggesting that they are functional. Presumably, these lectin domain-containing proteins can still bind carbohydrate ligands but their downstream actions do not rely on phosphorylation activity.
Functional implication of PtLecRLKs
LecRLKs are specifically present in the plant kingdom. To date, no homologs of LecRLKs have been reported in the genomes of fungus and human. LecRLKs are known to play roles in plant development, innate immunity [17, 20] and abiotic responses [41–43]. For example, Pi-d2, a rice G-type, and NbLecRK, a tomato L-type LecRLK, were shown to play a role in plant defense against a fungal pathogen and Phytophthora, respectively [9, 44]. Three tandem repeat LecRLK genes in Arabidopsis were shown to function redundantly to regulate abscisic acid response in seed germination . Two L-type LecRLKs, LecRK-IX.1 and LecRK-IX.2, regulate phytophthora resistance and cell death in Arabidopsis . A G-type LecRLK in Arabidopsis was shown to sense lipopolysaccharide, a potent microbe-associated molecular patterns from Gram-negative Pseudomonas and Xanthomonas . Recently, one L-type LecRLK in Arabidopsis was shown to function as a receptor for perceiving extracellular ATP . A cluster of G-type LecRLKs in rice was shown to function together to confer broad-spectrum and durable insect resistance . In our study, drastic number of PtLecRLKs was expressed in root tissues (Fig. 7 and Table 3). Root serves as a front barrier as well as an interface for various soil microbes including bacteria, fungus, protozoa and nematodes. These root-expressed PtLecRLKs have the potential to function as receptors for perceiving signals from soil microbes. In addition, approximately 50 % of PtLecRLK genes were expressed at very low or undetectable level in leaf, stem and root under normal conditions (Fig. 7), implying that the expression of these PtLecRLKs may depend on biotic or abiotic stimuli not contained in the current tested tissues and organs or developmental stage tissues. Because no functional characterization of any PtLecRLKs has been reported to date, this represents a fruitful area for further investigation.
We have reported the genome-wide identification of LecRLKs in the perennial woody model plant Populus. We uncovered that the LecRLK family has expanded in Populus. Through transcriptomics analysis, we identified a number of tissue-specific PtLecRLK genes. This study provides a foundation for functional characterization of this important family of receptor-like kinases.
- EGF domain:
Epidermal growth factor (EGF) domain
Fragments per kilobase of transcript per million mapped reads
Lectin receptor-like kinase
- PAN domain:
Plasminogen/apple/nematode (PAN) domain
Shiu SH, Bleecker AB. Expansion of the receptor-like kinase/Pelle gene family and receptor-like proteins in Arabidopsis. Plant Physiol. 2003;132:530–43.
Shiu SH, Karlowski WM, Pan R, Tzeng YH, Mayer KF, Li WH. Comparative analysis of the receptor-like kinase family in Arabidopsis and rice. Plant Cell. 2004;16:1220–34.
Li J, Chory J. A putative leucine-rich repeat receptor kinase involved in brassinosteroid signal transduction. Cell. 1997;90:929–38.
Clark SE, Williams RW, Meyerowitz EM. The CLAVATA1 gene encodes a putative receptor kinase that controls shoot and floral meristem size in Arabidopsis. Cell. 1997;89:575–85.
Elola MT, Blidner AG, Ferragut F, Bracalente C, Rabinovich GA. Assembly, organization and regulation of cell-surface receptors by lectin-glycan complexes. Biochem J. 2015;469:1–16.
Liu Y, Liu J, Pang X, Liu T, Ning Z, Cheng G. The roles of direct recognition by animal lectins in antiviral immunity and viral pathogenesis. Molecules. 2015;20:2272–95.
Navarro-Gochicoa MT, Camut S, Timmers AC, Niebel A, Herve C, Boutet E, Bono JJ, Imberty A, Cullimore JV. Characterization of four lectin-like receptor kinases expressed in roots of Medicago truncatula. Structure, location, regulation of expression, and potential role in the symbiosis with Sinorhizobium meliloti. Plant Physiol. 2003;133:1893–910.
Vaid N, Pandey PK, Tuteja N. Genome-wide analysis of lectin receptor-like kinase family from Arabidopsis and rice. Plant Mol Biol. 2012;80:365–88.
Wang Y, Weide R, Govers F, Bouwmeester K. L-type lectin receptor kinases in Nicotiana benthamiana and tomato and their role in Phytophthora resistance. J Exp Bot. 2015;66:6731–43.
Zhang X, Wang L, Yuan Y, Tian D, Yang S. Rapid copy number expansion and recent recruitment of domains in S-receptor kinase-like genes contribute to the origin of self-incompatibility. FEBS J. 2011;278:4323–37.
Barre A, Hervé C, Lescure B, Rougé R. Lectin receptor kinases in plants. Crit Rev Plant Sci. 2002;21:379–99.
Liu Y, Wu H, Chen H, Liu Y, He J, Kang H, Sun Z, Pan G, Wang Q, Hu J, et al. A gene cluster encoding lectin receptor kinases confers broad-spectrum and durable insect resistance in rice. Nat Biotechnol. 2015;33:301–5.
Stein JC, Howlett B, Boyes DC, Nasrallah ME, Nasrallah JB. Molecular cloning of a putative receptor protein kinase gene encoded at the self-incompatibility locus of Brassica oleracea. Proc Natl Acad Sci U S A. 1991;88:8816–20.
Stein JC, Dixit R, Nasrallah ME, Nasrallah JB. SRK, the stigma-specific S locus receptor kinase of Brassica, is targeted to the plasma membrane in transgenic tobacco. Plant Cell. 1996;8:429–45.
Kachroo A, Schopfer CR, Nasrallah ME, Nasrallah JB. Allele-specific receptor-ligand interactions in Brassica self-incompatibility. Science. 2001;293:1824–6.
Takasaki T, Hatakeyama K, Suzuki G, Watanabe M, Isogai A, Hinata K. The S receptor kinase determines self-incompatibility in Brassica stigma. Nature. 2000;403:913–6.
Vaid N, Macovei A, Tuteja N. Knights in action: lectin receptor-like kinases in plant development and stress responses. Mol Plant. 2013;6:1405–18.
Naithani S, Chookajorn T, Ripoll DR, Nasrallah JB. Structural modules for receptor dimerization in the S-locus receptor kinase extracellular domain. Proc Natl Acad Sci U S A. 2007;104:12211–6.
Hervé C, Serres J, Dabos P, Canut H, Barre A, Rougé P, Lescure B. Characterization of the Arabidopsis lecRK-a genes: members of a superfamily encoding putative receptors with an extracellular domain homologous to legume lectins. Plant Mol Biol. 1999;39:671–82.
Singh P, Zimmerli L. Lectin receptor kinases in plant innate immunity. Front Plant Sci. 2013;4:124.
André S, Siebert HC, Nishiguchi M, Tazaki K, Gabius HJ. Evidence for lectin activity of a plant receptor-like protein kinase by application of neoglycoproteins and bioinformatic algorithms. Biochim Biophys Acta. 1725;2005:222–32.
Nishiguchi M, Yoshida K, Sumizono T, Tazaki K. A receptor-like protein kinase with a lectin-like domain from lombardy poplar: gene expression in response to wounding and characterization of phosphorylation activity. Mol Genet Genomics. 2002;267:506–14.
Zuo K, Zhao J, Wang J, Sun X, Tang K. Molecular cloning and characterization of GhlecRK, a novel kinase gene with lectin-like domain from Gossypium hirsutum. DNA Seq. 2004;15:58–65.
GoodStein D, Shu S, Howson R, Neupane R, Hayes R, Fazo J, Mitros T, Dirks W, Hellsten U, Putnam N, Rokhsar D. Phytozome: a comparative platform for green plant genomics. Nucleic Acid Res. 2012;40:D1178–86.
Sundell D, Mannapperuma C, Netotea S, Delhomme N, Lin YC, Sjodin A, Van de Peer Y, Jansson S, Hvidsten TR, Street NR. The Plant Genome Integrative Explorer Resource: PlantGenIE.org. New Phytol. 2015;208:1149–56.
Finn RD, Bateman A, Clements J, Coggill P, Eberhardt RY, Eddy SR, Heger A, Hetherington K, Holm L, Mistry J, et al. Pfam: the protein families database. Nucleic Acids Res. 2014;42:D222–30.
Sigrist CJ, de Castro E, Cerutti L, Cuche BA, Hulo N, Bridge A, Bougueleret L, Xenarios I. New and continuing developments at PROSITE. Nucleic Acids Res. 2013;41:D344–7.
Mitchell A, Chang HY, Daugherty L, Fraser M, Hunter S, Lopez R, McAnulla C, McMenamin C, Nuka G, Pesseat S, et al. The InterPro protein families database: the classification resource after 15 years. Nucleic Acids Res. 2015;43:D213–21.
Krogh A, Brown M, Mian I, Sjolander K, Haussler D. Hidden Markov Models in computational Biology : Applocations to protein modeling. J Mol Biol. 1994;235:1501–31.
Krogh A, Larsson B, von Heijne G, Sonnhammer EL. Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J Mol Biol. 2001;305:567–80.
Petersen TN, Brunak S, von Heijne G, Nielsen H. SignalP 4.0: discriminating signal peptides from transmembrane regions. Nat Methods. 2011;8:785–6.
Edgar R. MUSCLE: multiple sequence alignment with high accuracy and high throuput. Nucleic Acid Res. 2004;32:1792–7.
Kumar S, Stecher G, Tamura K. MEGA7: Molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 2016;33:1870–4.
Guindon S, Dufayar JF, Lefort V, Anisimova M, Hordijk W, Gascuel O. New Algorithms and methods to estimate maximum-likelihood phylogenies: Assessing the performance of PhyML 3.0. Syst Biol. 2010;59:307–21.
Wickham H. ggplot2: elegant graphics for data analysis. New York: Springer-Verlag; 2009.
Hofberger JA, Nsibo DL, Govers F, Bouwmeester K, Schranz ME. A complex interplay of tandem- and whole-genome duplication drives expansion of the L-type lectin receptor kinase gene family in the brassicaceae. Genome Biol Evol. 2015;7:720–34.
Bouwmeester K, Govers F. Arabidopsis L-type lectin receptor kinases: phylogeny, classification, and expression profiles. J Exp Bot. 2009;60:4383–96.
Ranf S, Gisch N, Schäffer M, Illig T, Westphal L, Knirel YA, Sánchez-Carballo PM, Zahringer U, Hückelhoven R, Lee J, Scheel D. A lectin S-domain receptor kinase mediates lipopolysaccharide sensing in Arabidopsis thaliana. Nat Immunol. 2015;16:426–33.
Cui Y, Bi Y, Brugiere N, Arnoldo M, Rothstein S. The S locus glycoprotein and S receptor kinase are sufficient for self-pollen rejection in Brassica. Proc Natl Acad Sci. 2000;97:3713–7.
Tuskan GA, Difazio S, Jansson S, Bohlmann J, Grigoriev I, Hellsten U, Putnam N, Ralph S, Rombauts S, Salamov A, et al. The genome of black cottonwood, Populus trichocarpa (Torr. & Gray). Science. 2006;313:1596–604.
Sun XL, Yu QY, Tang LL, Ji W, Bai X, Cai H, Liu XF, Ding XD, Zhu YM. GsSRK, a G-type lectin S-receptor-like serine/threonine protein kinase, is a positive regulator of plant tolerance to salt stress. J Plant Physiol. 2013;170:505–15.
Xin Z, Wang A, Yang G, Gao P, Zheng ZL. The Arabidopsis A4 subfamily of lectin receptor kinases negatively regulates abscisic acid response in seed germination. Plant Physiol. 2009;149:434–44.
Deng K, Wang Q, Zeng J, Guo X, Zhao X, Tang D, Liu X. A lectin receptor kinase positively regulates ABA response during seed germination and is involved in salt and osmotic stress response. J Plant Biol. 2009;52:493–500.
Chen X, Shang J, Chen D, Lei C, Zou Y, Zhai W, Liu G, Xu J, Ling Z, Cao G, et al. A B-lectin receptor kinase gene conferring rice blast resistance. Plant J. 2006;46:794–804.
Wang Y, Cordewener JH, America AH, Shan W, Bouwmeester K, Govers F. Arabidopsis Lectin Receptor Kinases LecRK-IX.1 and LecRK-IX.2 Are Functional Analogs in Regulating Phytophthora Resistance and Plant Cell Death. Mol Plant Microbe Interact. 2015;28:1032–48.
Choi J, Tanaka K, Cao Y, Qi Y, Qiu J, Liang Y, Lee SY, Stacey G. Identification of a plant receptor for extracellular ATP. Science. 2014;343:290–4.
This work was supported by the Plant-Microbe Interfaces Scientific Focus Area in the Genomic Science Program, the Office of Biological and Environmental Research in the U.S. Department of Energy Office of Science. Oak Ridge National Laboratory is managed by UT-Battelle, LLC, for the U.S. Department of Energy under contract DE-AC05-00OR22725. The work conducted by the U.S. Department of Energy Joint Genome Institute was supported by the Office of Science of the US Department of Energy under contract number DE-AC02-05CH11231.
The funding bodies have no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Availability of data and materials
The transcriptomics data discussed in this publication are accessible through the U.S. Department of Energy Joint Genome Institute’s Phytozome (http://phytozome.jgi.doe.gov/pz/portal.html). Phylogenetic data have been deposited to TreeBase and are accessible via the URL: http://purl.org/phylo/treebase/phylows/study/TB2:S19725. Additional supporting data are included as additional files.
Experiments in this study were conceived by YY, JS, GAT and JGC. Experiments were performed by YY, SJ, MK, JJ, AS and JGC. Data analysis was performed by YY, SJ, MK, JJ, AS and JGC. All authors participated in editing the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
The sequences of primers used for RT-PCR analysis in this study. (XLSX 8 kb)
List of lectin domain-containing Populus proteins that lack the protein kinase domain. (XLSX 11 kb)
Comparison of different types of PtLecRLKs. (A) Amino acid sequence alignment of randomly selected PtLecRLKs from each type by ClustalW. Amino acid identity is displayed by green color above the first row in the plot. Note that the protein kinase domains at the C-terminus are highly conserved whereas lectin domains at the N-terminus are very distinct. (B) Phylogenetic tree using neighbor joining method with 1000 bootstrapping of the randomly selected PtLecRLKs. Note that three types are separated clearly. The number on branch indicates bootstrapping value of each node formation. (C) The amino acid sequence identity of examined PtLecRLKs. (PPTX 477 kb)
List of G-type PtLecRLKs. (XLSX 23 kb)
List of L-type PtLecRLKs. (XLSX 14 kb)
List of C-type PtLecRLK. (XLSX 9 kb)
List of G-, L- and C-type LecRLKs in moss, shrub, corn, soybean and Eucalyptus. (XLSX 18 kb)
Phylogenetic analysis of G- and L-type PtLecRLKs together with Arabidopsis LecRLKs using neighbor-joining method with 1000 bootstrap resampling. (A) Phylogenetic tree of G-type LecRLKs. The groups are marked by the same classification shown in Fig. 3a. (B) Phylogenetic tree of L-type LecRLKs. The groups are marked by the same classification shown in Fig. 3b. Number on the each node indicates the bootstrap value for each node formation. (TIF 7638 kb)
Phylogenetic tree analysis of LecRLKs from Populus, Eucalyptus, Arabidopsis and rice using neighbor joining method with 1000 bootstrap. Numbers on the node indicate the bootstrap value for each node formation. (A) Phylogenetic tree of G-type LecRLKs. Groups are marked by the same classification shown in Fig. 4a. (B) Phylogenetic tree of L-type LecRLKs. Groups are marked by the same classification shown in Fig. 4b. Convergent clade of L-type EgLecRLKs is highlighted by light red color. The blue highlighted nodes contain only rice LecRLKs. (C) Phylogenetic tree of the C-type LecRLKs. (TIF 9324 kb)
The amino acid sequence alignment and conserved motifs of G-type PtLecRLKs. (A) Amino acid sequence alignment via CLUSTALW. To determine conserved amino acid regions, 50 % sequence identity was used as a cutoff. Note that the amino acid sequence in the protein kinase domain is highly conserved in most G-type PtLecRLKs whereas the other domains such as S-locus glycoprotein, EGF, PAN, TM and signal peptide varied. Highly conserved motifs are boxed with labels a, b, c, d and e. The red arrows indicate truncated bulb lectin domains. The blue arrows indicate the truncated protein kinase domains. (B) The conserved motif sequences marked on panel A. Sequence logo was generated from the consensus amino acid sequence over 50 % sequence identity. (PPTX 3107 kb)
The amino acid sequence alignment and conserved motifs of L-type PtLecRLKs. (A) Amino acid sequence alignment via CLUSTALW. Amino acid sequence identity of 50 % was used to determine cluster of protein domain and phylogenetic node of 50 L-type PtLecRLKs. The red arrows indicate truncated legume lectin domains. The blue arrows indicate the truncated protein kinase domains. (B) The conserved motifs marked in panel A. Sequence logo was generated from the consensus amino acid sequence over 50 % sequence identity. (PPTX 3150 kb)
Transcript level of G-type PtLecRLK genes in 24 different datasets from the Populus Gene Atlas Study. RNA-seq data were collected from the Populus Gene Atlas Study in Phytozome v11.0 (http://phytozome.jgi.doe.gov/pz/portal.html). The transcript levels for each gene were expressed as FPKM. The excel sheet labeled as “whole_set” contains the original FPKM values from Gene Atlas. The data of four different tissues under standard condition are sorted in the data sheet labeled as “standard”. The group number is listed in the first column of standard datasheet based on Fig. 3 phylogenetic tree analysis result. (XLSX 62 kb)
Transcript level of L-type PtLecRLK genes in 24 different datasets from the Populus Gene Atlas Study. RNA-seq data were collected from the Populus Gene Atlas Study in Phytozome v11.0 (http://phytozome.jgi.doe.gov/pz/portal.html). The transcript levels for each gene were expressed as FPKM. The sheet labeled as “whole_set” contains the original FPKM values from Gene Atlas. The data of four different tissues under standard condition are sorted in the data sheet labeled as “standard”. The group number is listed in the first column of standard datasheet based on Fig. 3 phylogenetic tree analysis result. (XLSX 24 kb)
Transcript level of C-type PtLecRLK gene in 24 different datasets from the Populus Gene Atlas Study. RNA-seq data were collected from the Populus Gene Atlas Study in Phytozome v11.0 (http://phytozome.jgi.doe.gov/pz/portal.html). The transcript level was expressed as FPKM. The sheet labeled as “whole_set” contains the original FPKM values from Gene Atlas. The data of four different tissues under standard condition are sorted in the data sheet labeled as “standard”. (XLSX 10 kb)
List of PtLecRLK genes expressed specifically in roots. RNA-seq data were collected from the Populus Gene Atlas Study in Phytozome v11.0 (http://phytozome.jgi.doe.gov/pz/portal.html). (XLSX 12 kb)
Expression patterns of PtLecRLK genes in the reproductive tissues and organs. RNA-seq data were collected from the Populus Gene Atlas Study in Phytozome v11.0 (http://phytozome.jgi.doe.gov/pz/portal.html). The FPKM value of three female genotypes and three male genotypes were used to generate the heatmaps. The tissue specificity of gene expression was determined by the comparison of FPKM value ≥ 1 in a given plant versus FPKM < 1 in plants with opposite sex. Three different zones were categorized (Female: transcript only detected in at least one female plant but not in any male plants; Male: transcript only detected in at least one male plant but not in any female plants; Both: transcript detected in both female and male plants). (A) The expression patterns of the G-type PtLecRLK genes. (B) The expression patterns of the L-type PtLecRLK genes. (C) The expression pattern of the C-type PtLecRLK gene. (PPTX 9960 kb)
List of PtLecRLK genes expressed in the female and male reproductive tissues/organs. RNA-seq data were collected from the Populus Gene Atlas Study in Phytozome v11.0 (http://phytozome.jgi.doe.gov/pz/portal.html). (XLSX 24 kb)
The distribution of number of PtLecRLKs from each group in different tissues and organs. (DOCX 48 kb)
Diagrams of protein domain architecture of lectin domain-containing proteins that lack the protein kinase domain in Populus. (PPTX 63 kb)
About this article
Cite this article
Yang, Y., Labbé, J., Muchero, W. et al. Genome-wide analysis of lectin receptor-like kinases in Populus . BMC Genomics 17, 699 (2016). https://doi.org/10.1186/s12864-016-3026-2
- Lectin domain
- Lectin receptor-like kinase (LecRLK)
- Perennial woody plant
- Receptor like-kinase (RLK)
- Transmembrane kinase